ABCC10
ATP-binding cassette, sub-family C (CFTR/MRP), member 10 | |||||||||||||
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Identifiers | |||||||||||||
Symbols | ABCC10 ; EST182763; MRP7; SIMRP7 | ||||||||||||
External IDs | OMIM: 612509 MGI: 2386976 HomoloGene: 58616 GeneCards: ABCC10 Gene | ||||||||||||
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RNA expression pattern | |||||||||||||
More reference expression data | |||||||||||||
Orthologs | |||||||||||||
Species | Human | Mouse | |||||||||||
Entrez | 89845 | 224814 | |||||||||||
Ensembl | ENSG00000124574 | ENSMUSG00000032842 | |||||||||||
UniProt | Q5T3U5 | Q8R4P9 | |||||||||||
RefSeq (mRNA) | NM_001198934 | NM_145140 | |||||||||||
RefSeq (protein) | NP_001185863 | NP_660122 | |||||||||||
Location (UCSC) |
Chr 6: 43.43 – 43.45 Mb |
Chr 17: 46.3 – 46.33 Mb | |||||||||||
PubMed search | |||||||||||||
Multidrug resistance-associated protein 7 is a protein that in humans is encoded by the ABCC10 gene.[1][2]
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This ABC full-transporter is a member of the MRP subfamily which is involved in multi-drug resistance. Alternative splicing of this gene results in multiple transcript variants; however, not all variants have been fully described.[2]
See also
References
- ↑ Allikmets R, Gerrard B, Hutchinson A, Dean M (Feb 1997). "Characterization of the human ABC superfamily: isolation and mapping of 21 new genes using the expressed sequence tags database.". Hum Mol Genet 5 (10): 1649–55. doi:10.1093/hmg/5.10.1649. PMID 8894702.
- 1 2 "Entrez Gene: ABCC10 ATP-binding cassette, sub-family C (CFTR/MRP), member 10".
Further reading
- Hopper E, Belinsky MG, Zeng H; et al. (2001). "Analysis of the structure and expression pattern of MRP7 (ABCC10), a new member of the MRP subfamily.". Cancer Lett. 162 (2): 181–91. doi:10.1016/S0304-3835(00)00646-7. PMID 11146224.
- Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Chen ZS, Hopper-Borge E, Belinsky MG; et al. (2003). "Characterization of the transport properties of human multidrug resistance protein 7 (MRP7, ABCC10).". Mol. Pharmacol. 63 (2): 351–8. doi:10.1124/mol.63.2.351. PMID 12527806.
- Kao HH, Chang MS, Cheng JF, Huang JD (2003). "Genomic structure, gene expression, and promoter analysis of human multidrug resistance-associated protein 7.". J. Biomed. Sci. 10 (1): 98–110. doi:10.1159/000068078. PMID 12566991.
- Mungall AJ, Palmer SA, Sims SK; et al. (2003). "The DNA sequence and analysis of human chromosome 6.". Nature 425 (6960): 805–11. doi:10.1038/nature02055. PMID 14574404.
- Ota T, Suzuki Y, Nishikawa T; et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Hopper-Borge E, Chen ZS, Shchaveleva I; et al. (2004). "Analysis of the drug resistance profile of multidrug resistance protein 7 (ABCC10): resistance to docetaxel.". Cancer Res. 64 (14): 4927–30. doi:10.1158/0008-5472.CAN-03-3111. PMID 15256465.
- Wooden SL, Kalb SR, Cotter RJ, Soloski MJ (2005). "Cutting edge: HLA-E binds a peptide derived from the ATP-binding cassette transporter multidrug resistance-associated protein 7 and inhibits NK cell-mediated lysis.". J. Immunol. 175 (3): 1383–7. doi:10.4049/jimmunol.175.3.1383. PMID 16034073.
- Naramoto H, Uematsu T, Uchihashi T; et al. (2007). "Multidrug resistance-associated protein 7 expression is involved in cross-resistance to docetaxel in salivary gland adenocarcinoma cell lines.". Int. J. Oncol. 30 (2): 393–401. doi:10.3892/ijo.30.2.393. PMID 17203221.
External links
- ABCC10 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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